95.6K
THDay 24: posting a video every day in May for ALS Awareness
@thekaregiver
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#Alsawareness
Guarda 184K video Reel su Alsawareness da persone di tutto il mondo.
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19.7K
AMwith all the money pharma has they still haven’t been able to figure out decent tasting medication
follow @alsnewstoday to raise awareness and support ALS
#alsawareness #lougherigsdisease #raredisease #disabledlife #braindisease #disabilityrepresentation #terminallyill #ad #chroniccondition #rarediseasecommunity #alsnewstoday
@amandatam00
239.3K
DAALS isn’t popular. It doesn’t trend. It doesn’t go viral. And that’s exactly why I’m talking about it anyway.
Amyotrophic lateral sclerosis is a terminal, progressive neurodegenerative disease that slowly takes away mobility, speech, swallowing, and eventually breathing. It’s also known as Lou Gehrig’s disease, motor neuron disease, or MND. Different names. Same devastating reality.
I share ALS awareness even when it feels uncomfortable, inconvenient, or easy to scroll past. Because behind every diagnosis is a real person, a family learning a new language of loss, and a life that changed without warning.
ALS doesn’t care about algorithms. It doesn’t care about trends. And it definitely doesn’t wait for attention. Awareness matters because early symptoms are often missed. Awareness matters because caregivers need support. Awareness matters because funding research starts with people actually knowing what ALS is.
This video isn’t about chasing views. It’s about visibility. It’s about saying the name of the disease out loud. It’s about reminding people that rare doesn’t mean insignificant, and quiet suffering still deserves to be seen.
If you or someone you love is living with ALS, amyotrophic lateral sclerosis, motor neuron disease (MND), or Lou Gehrig’s disease, you are not invisible. And if you don’t know much about ALS yet, this is your invitation to learn, listen, and help spread awareness.
Sometimes the most important stories aren’t the popular ones. They’re the ones that need a voice.
@darin_nakakihara
2.1K
BEALS AWARENESS
#havingfun #alsawareness #alswarrior #silly #laughteristhebestmedicine💊 #husband #noharmdone
@bethsteckerreed
25.7K
PA“Familia y Amigos, disfrutemos de la vida” es el mensaje que le manda Eli a todos en estas fiestas de fin de año 🏖️
@coco__reynolds
#pasionporvivir #ela #alsawareness #love #amor
@pasionporvivirpty
40.3K
ALNothing better than this!
@silverts_adaptive also this dress is by far the cutest most functional adaptive clothing ever. Definitely recommend.
#als #heralsstory #lou #lougherigsdisease #alsadvocacy #alsiseverywhere #cure #alscaregivers #alsawareness #lougehrigs
@alswithsalym
155.5K
BYGeorge Strait Takes the ALS Ice Bucket Challenge! You're Next!
George Strait accepts the ALS Ice Bucket Challenge! Watch George nominate Martina McBride, Governor Rick Perry, and Dean Dillon. Join us in supporting ALS awareness and research. #ALSChallenge #IceBucketChallenge #ALSicebucketchallenge #GeorgeStrait #MartinaMcBride #RickPerry #DeanDillon #ChallengeAccepted #ALSFoundation #Charity #ViralChallenge #IceBucket
@bytesizen
206.2K
CIEric Dane passed away on February 19, 2026, at the age of 53, after a courageous battle with amyotrophic lateral sclerosis
Dane became a household name through a string of memorable and iconic roles. He broke out as Dr. Mark "McSteamy" Sloan on the long-running medical drama Grey's Anatomy, a role that turned him into a fan favorite and helped define his career. He also earned critical acclaim for portraying Cal Jacobs on HBO's hit series Euphoria, a complex character whose storylines resonated with audiences and showcased Dane's range as an actor. Dane's death came about 10 months after publicly announcing his ALS diagnosis, during which time he became a passionate advocate for ALS awareness and research using his platform to help others facing the disease.
Pulp Tart would like to thank Eric Dane for all of his incredible work and the unforgettable characters he brought to life. His talent, presence, and impact on television will not be forgotten. We send our deepest condolences to his loved ones, friends, and fans during this difficult time.🤍
Credits: @rtwtofficial
@cinematricss
25.1K
ALIt’s hard to believe it’s been 11 years since the Ice Bucket Challenge took the world by storm! In the summer of 2014, millions dumped buckets of ice water over their heads—and in doing so, helped raise over $220 million for ALS research, patient services, and advocacy efforts. ALS TDI alone received more than $4 million, fueling critical research that continues to this day.
One of the most powerful voices behind the challenge was Anthony Carbajal. His heartfelt viral video and subsequent unforgettable moment on The Ellen Show helped put ALS and ALS TDI in the global spotlight.
Earlier this year, we sat down with Anthony to reflect on the movement that changed everything—and the lasting impact it has on ALS awareness and research.
Read more about his story and the legacy of the Ice Bucket Challenge here:
🔗 https://www.als.net/news/anthony-carbajal-on-the-als-ice-bucket-challenge/
@alstdi
209.8K
TI9 months - that was all the time the world had between his brave confession and his final public smile.🩺💔
When Eric Dane stepped forward to reveal his ALS diagnosis, he did not hide behind silence or retreat from the cameras; instead, he stood there with the same quiet intensity that once made Dr. Mark Sloan unforgettable on Grey's Anatomy, only this time there was no script, no lighting team, no second take just a man facing the most difficult chapter of his life with dignity.
That first appearance after his announcement carried a weight that words could barely hold. His smile was softer, his frame slightly thinner, yet his eyes still carried warmth, still carried gratitude for the fans who had followed him from Seattle Grace to the complicated world of Euphoria, where he portrayed a father layered with flaws and humanity.
Across those 9 months, every sighting felt different. Every step onto a red carpet seemed slower, every wave to the crowd more intentional, as if he understood that time was no longer stretching endlessly ahead of him but narrowing into precious moments. The cameras captured his courage, yet what they truly documented was love — love from friends who stood close, love from his daughters who remained his greatest pride, love from a family determined to protect his peace while the world watched.
Then came the last time we saw him in public. There was no grand farewell, no dramatic goodbye speech, just another appearance that now feels sacred in hindsight. No one knew it would be the final image the final glimpse of the man who once lit up hospital corridors on television and later turned personal pain into advocacy for ALS awareness.
And now, he is gone.
Gone from premieres, gone from interviews, gone from the flashing lights yet impossible to erase. His journey from that first brave admission to his final public moment lasted only nine months, but within that brief span he showed what resilience truly looks like. He did not allow illness to silence his presence. He did not let fear define his legacy.
Today, there is an aching stillness where his appearances once were. Fans scroll back to photos, replay interviews, hold onto clips as i
@tinaskia_chinel
169.4K
ALThis is ALS Awareness: elevator breaks what do you do? For most you’re annoyed and take the stairs, for others it’s a 30 minute long marathon to get up, a call to the fire department to be lifted up. Being without the 400 pound chair that you rely on for independence.
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#alsawareness #fuckals #als #endals #alsadvocacy #alssucks #terminalillness #mnd #love #family #alsawarenessmonth
@alliecbrunner
266
SY"ALS warriors: fighting For a cure, living with courage "
Physiotherapy can play a crucial role in managing the symptoms of Amyotrophic Lateral Sclerosis (ALS) and improving the quality of life for individuals with this condition.
Benefits of Physiotherapy in ALS:
1. Maintaining mobility and flexibility: Physiotherapy can help slow down the progression of muscle weakness and stiffness, allowing individuals to maintain their mobility and flexibility for as long as possible.
2. Improving balance and reducing fall risk: Physiotherapists can provide exercises and strategies to improve balance and reduce the risk of falls, which is essential for individuals with ALS who may experience muscle weakness and coordination problems.
3. Enhancing respiratory function: Physiotherapy can help improve lung function and increase oxygenation, which is critical for individuals with ALS who may experience respiratory muscle weakness.
4. Managing pain and discomfort: Physiotherapists can provide pain-relieving techniques, such as massage, heat, or cold therapy, to help manage pain and discomfort associated with ALS.
5. Improving overall quality of life: Physiotherapy can help individuals with ALS maintain their independence, participate in activities they enjoy, and improve their overall quality of life.
#ALS awareness
#ALS research
#ALS support
#lougehrigs disease
#motoneuron disease
@syedphysiotherapyclinicambur
✨ Guida alla Scoperta #Alsawareness
Instagram ospita 184K post sotto #Alsawareness, creando uno degli ecosistemi visivi più vivaci della piattaforma.
#Alsawareness è uno dei trend più coinvolgenti su Instagram in questo momento. Con oltre 184K post in questa categoria, creator come @darin_nakakihara, @tinaskia_chinel and @cinematricss stanno guidando la strada con i loro contenuti virali. Esplora questi video popolari in modo anonimo su Pictame.
Cosa è di tendenza in #Alsawareness? I video Reels più visti e i contenuti virali sono in evidenza sopra.
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💡 I contenuti top ottengono oltre 10K visualizzazioni - concentrati sui primi 3 secondi
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